NCT03901521Enrolling by invitation
Autosomal Dominant Polycystic Kidney Disease Somatic Mutation Biorepository
Source: ClinicalTrials.gov · Last updated 22 Jan 2026
Brief summary (registry, in English)
This study will analyze the germline and somatic mutations underlying the development of ADPKD in order to better understand the genetic mechanism responsible for the cystic transformation. Once identified, these mutations could help us understand better the mechanism leading to the development of this disease and may explain at least in part the phenotypic variability.
- Status (registry)
- Enrolling by invitation
- Study type
- Observational
- Enrollment
- 100 (estimated)
- First submitted
- 13 Mar 2019
- Start date
- 1 Jun 2018
- Primary completion date
- 31 Dec 2028
- Lead sponsor
- Weill Medical College of Cornell University
- Diseases
- Polycystic kidney disease
- NCT number
- NCT03901521
What you commit to
- Study type: Observational
- Planned participants: 100
- From 1 Jun 2018 to the primary completion date, 31 Dec 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Unable or unwilling to provide informed consent
Who the study is looking for
- Males or females
- 18 years of age or older
- Confirmed diagnosis of ADPKD
- Undergoing a native nephrectomy
- Willing and able to provide informed consent
Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Weill Cornell Medicine Coordinator of this site? Confirm its status | New York | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.